Product Details

SNP ID

rs201000185

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:48029530 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGGCGCTGCCAGGAAGTGCTTGGC[A/G]GGGCTGGGGCCCGGGAGGCACACAG

Phenotype

MIM: 616591

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ZBTB7C PubMed Links

Gene Details

Gene

ZBTB7C

Gene Name

zinc finger and BTB domain containing 7C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039360.2	2303	Silent Mutation	CCC,CCT	P530P	NP_001034449.1
NM_001318841.1	2303	Silent Mutation	CCC,CCT	P530P	NP_001305770.1
XM_005258229.4	2303	Silent Mutation	CCC,CCT	P530P	XP_005258286.1
XM_011525861.2	2303	Silent Mutation	CCC,CCT	P579P	XP_011524163.1
XM_011525863.2	2303	Silent Mutation	CCC,CCT	P539P	XP_011524165.1
XM_011525864.2	2303	Silent Mutation	CCC,CCT	P539P	XP_011524166.1
XM_011525865.2	2303	Silent Mutation	CCC,CCT	P539P	XP_011524167.1
XM_011525866.2	2303	Silent Mutation	CCC,CCT	P539P	XP_011524168.1
XM_011525867.2	2303	Silent Mutation	CCC,CCT	P539P	XP_011524169.1
XM_011525869.2	2303	Silent Mutation	CCC,CCT	P538P	XP_011524171.1
XM_011525870.2	2303	Silent Mutation	CCC,CCT	P530P	XP_011524172.1
XM_011525871.2	2303	Silent Mutation	CCC,CCT	P530P	XP_011524173.1
XM_017025605.1	2303	Silent Mutation	CCC,CCT	P579P	XP_016881094.1
XM_017025606.1	2303	Silent Mutation	CCC,CCT	P539P	XP_016881095.1
XM_017025607.1	2303	Silent Mutation	CCC,CCT	P539P	XP_016881096.1
XM_017025608.1	2303	Silent Mutation	CCC,CCT	P538P	XP_016881097.1
XM_017025609.1	2303	Silent Mutation	CCC,CCT	P530P	XP_016881098.1

View Full Product Details